MnMX (M = Co or Ni, X = Si or Ge) alloys with strong magnetostructural coupling exhibit giant magnetic entropy change and are currently extensively studied. However, large thermal hysteresis results in serious irreversibility of the magnetocaloric effect in this well-known system. In this work, we report a low thermal hysteresis and large reversible magnetocaloric effect in a MnNiGe-based system. The introduction of Fe into both Ni and Mn sites can establish stable magnetostructural transitions from paramagnetic hexagonal to ferromagnetic orthorhombic phases. Fascinatingly, a low thermal hysteresis of 5.2 K is achieved in Mn0.9Fe0.2Ni0.9Ge alloy with a large magnetization difference of 62.1 A m2/kg between the two phases. These optimized parameters lead to a partially reversible phase transformation under a magnetic stimulus and bring about a large reversible magnetic entropy change of −18.6 Jkg−1K−1 under the field variation of 0–5 T, which is the largest value reported in MnMX system up to now. Moreover, this low-hysteresis magnetostructural transformation and large reversible magnetocaloric effect can be tuned by doping with Si in a wide temperature range covering room temperature. We also introduce geometrically nonlinear theory to discuss the origin of low hysteresis in MnMX alloys. A strong relation is found between thermal hysteresis and the change of c axis in the orthorhombic structure during the transition. Our work greatly develops the potential of MnMX alloys as magnetocaloric materials and is meaningful to seek or design a MnMX system with low thermal hysteresis.@en

The first-order magneto-elastic transition in the Mn–Fe–P–Si alloys can be tailored by vanadium substitution. Alloys with a suitable V substitution provide an excellent magnetocaloric effect with minor hysteresis in low magnetic fields up to 1.2 T. Mössbauer measurements show that the hyperfine field is reduced by V substitution. Neutron diffraction reveals that Fe is substituted by V on the 3f site and the magnetic moment on the 3f site is enhanced by the V substitution. The modified magnetic exchange field around the 3f and 3g positions in the lattice can be utilized to design suitable magnetocaloric materials that operate in low magnetic fields.@en

The influence of Nb substitution on the structure, magnetoelastic transition and magnetocaloric properties has been investigated for the Mn1.1Fe0.85-xNbxP0.43Si0.57 alloys. The substitution for Fe by merely 4.7 at.% Nb (i.e. x = 0.04) significantly diminishes the thermal hysteresis from 10 to 1 K due to the reduced structural discontinuity crossing the magnetoelastic transition. This also improves the mechanical stability. The Curie temperature of the magnetoelastic transition is lowered by approximately 11.6 K per at.% of the Nb substitution, originating from the enhanced covalent bonding that favors the paramagnetic state. The giant magnetocaloric effect is still retained in the Nb-substituted alloys.@en

Ni-Mn-X (X = In, Sn, and Sb) based Heusler alloys show a strong potential for magnetic refrigeration owing to their large magnetocaloric effect (MCE) associated with first-order magnetostructural transition. However, the irreversibility of the MCE under low field change of 0–1 T directly hinders its application as an efficient magnetic coolant. In this work, we systematically investigate thermal and magnetic properties, crystalline structure and magnetocaloric performance in Ni51−xMn33.4In15.6Vx alloys. With the introduction of V, a stable magnetostructural transition near room temperature is observed between martensite and austenite. An extremely small hysteresis of 2.3 K is achieved for the composition x = 0.3. Due to this optimization, the magneticfield induced structural transition is partially reversible under 0–1 T cycles, resulting in a reversible MCE. Both magnetic and calorimetric measurements consistently show that the largest value for the reversible magnetic entropy change can reach about 5.1 J kg−1 K−1 in a field change of 0–1 T. A considerable and reversible adiabatic temperature change of −1.2 K by the direct measurement is also observed under a field change of 0–1.1 T. Furthermore, the origin of this small hysteresis is discussed. Based on the lattice parameters, the transformation stretch tensor is calculated, which indicates an improved geometric compatibility between the two phases. Our work greatly improves the MCE performance of Ni-Mn-X-based alloys and make them suitable as realistic magnetic refrigeration materials. @en

The giant magnetocaloric effect is widely achieved in hexagonal MnMX-based (M = Co or Ni, X = Si or Ge) ferromagnets at their first-order magnetostructural transition. However, the thermal hysteresis and low sensitivity of the magnetostructural transition to the magnetic field inevitably lead to a sizeable irreversibility of the low-field magnetocaloric effect. Here, we show an alternative way to realize a reversible low-field magnetocaloric effect in MnMX-based alloys by taking advantage of the second-order phase transition. With introducing Cu into Co in stoichiometric MnCoGe alloy, the martensitic transition is stabilized at high temperature, while the Curie temperature of the orthorhombic phase is reduced to room temperature. As a result, a second-order magnetic transition with a negligible thermal hysteresis and a large magnetization change can be observed, enabling a reversible magnetocaloric effect. By both calorimetric and direct measurements, a reversible adiabatic temperature change of about 1 K is obtained under a field change of 0-1 T at 304 K, which is larger than that obtained in a first-order magnetostructural transition. To gain a better insight into the origin of these experimental results, first-principles calculations are carried out to characterize the chemical bonds and the magnetic exchange interaction. Our work provides an understanding of the MnCoGe alloy and indicates a feasible route to improve the reversibility of the low-field magnetocaloric effect in the MnMX system.@en